
Busse Hospital Disposables, Inc.
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BUSSE EPIDURAL CATHETER is an FDA 510(k)-cleared medical device (K070465) manufactured by Busse Hospital Disposables, Inc.. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 18, 2007. Regulation: 8.